A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176601



Internal ID20743642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124350293..124398055hg38UCSC Ensembl
chr9:127112572..127160334hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3847763
hg1947763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435798
Supporting Variants
Samples
Known GenesLOC100129034, NEK6, PSMB7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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